http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2704607-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-12
filingDate 1977-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3160e108eda0815a93e36ecb302ab019
publicationDate 1978-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2704607-A1
titleOfInvention PROCESS FOR MANUFACTURING FLUORINE KETONE
abstract Aliphatic perfluoroketones (I) are prepd. by reacting a perfluorocarboxylic acid salt R1-CO2M (II) with a perfluoroacyl fluoride R2-CO-F (III) in a polar aprotic solvent at 20-200 degrees C. In the formulae M is Li, Na, K, Rb, Cs or Ag; R1 is 2-50C perfluoroalkyl opt. contg. ether-O-function(s) R2 is 1-50C perfluoroalkyl opt. contg. ether-O-function(s). (II) may be prepd. from R1COF and a salt of formic or oxalic acid or of a Gp. IIIA to VIIA element oxyacid which is less strong than CF3CO2H, esp. M2CO3. Prepn. is in a polar aprotic solvent at 20-200 degrees C. Alternatively a mixt. of (II) and (III) may be prepd. from (R1CO)2O and an alkali metal fluoride. Perfluorolefins (which are difficult to obtain) are not used. High boiling (I) may be prepd. (I) are inert to acids, oxidants and heat. They may be used as heat transfer media or lubricants. In an example perfluoro-2,4-bis-(3,6-dimethyl-1,4-dioxanyl-2-oxylpentan-3-one was prepd. from potassium perfluoro- alpha-(3,6-dimethyl-1,4-dioxanyl-2-oxylpropionate and the corresp. perfluoroacyl fluoride in tetraglyme.
priorityDate 1977-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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